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Lukas Forer
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Next-generation genotype imputation service and methods
S Das, L Forer, S Schönherr, C Sidore, AE Locke, A Kwong, SI Vrieze, ...
Nature genetics 48 (10), 1284-1287, 2016
30802016
A reference panel of 64,976 haplotypes for genotype imputation
S McCarthy, S Das, W Kretzschmar, O Delaneau, AR Wood, A Teumer, ...
Nature Genetics 8 (10), 1279–1283, 2016
2802*2016
Reference-based phasing using the Haplotype Reference Consortium panel
PR Loh, P Danecek, PF Palamara, C Fuchsberger, Y A Reshef, ...
Nature genetics 48 (11), 1443-1448, 2016
14442016
Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program
D Taliun, DN Harris, MD Kessler, J Carlson, ZA Szpiech, R Torres, ...
Nature 590 (7845), 290-299, 2021
12532021
HaploGrep 2: mitochondrial haplogroup classification in the era of high-throughput sequencing
H Weissensteiner, D Pacher, A Kloss-Brandstätter, L Forer, G Specht, ...
Nucleic acids research 44 (W1), W58-W63, 2016
8142016
Mirror extreme BMI phenotypes associated with gene dosage at the chromosome 16p11. 2 locus
S Jacquemont, A Reymond, F Zufferey, L Harewood, RG Walters, ...
Nature 478 (7367), 97-102, 2011
5272011
The power of genetic diversity in genome-wide association studies of lipids
SE Graham, SL Clarke, KHH Wu, S Kanoni, GJM Zajac, S Ramdas, ...
Nature 600 (7890), 675-679, 2021
3542021
The GenomeAsia 100K Project enables genetic discoveries across Asia
Nature 576 (7785), 106-111, 2019
2762019
A saturated map of common genetic variants associated with human height
L Yengo, S Vedantam, E Marouli, J Sidorenko, E Bartell, S Sakaue, ...
Nature 610 (7933), 704-712, 2022
238*2022
Disease burden and risk profile in referred patients with moderate chronic kidney disease: composition of the German Chronic Kidney Disease (GCKD) cohort
S Titze, M Schmid, A Köttgen, M Busch, J Floege, C Wanner, ...
Nephrology Dialysis Transplantation 30 (3), 441-451, 2015
1802015
mtDNA-Server: next-generation sequencing data analysis of human mitochondrial DNA in the cloud
H Weissensteiner, L Forer, C Fuchsberger, B Schöpf, A Kloss-Brandstätter, ...
Nucleic acids research 44 (W1), W64-W69, 2016
1632016
Sensory phenotype and risk factors for painful diabetic neuropathy: a cross-sectional observational study
J Raputova, I Srotova, E Vlckova, C Sommer, N Üçeyler, F Birklein, ...
Pain 158 (12), 2340, 2017
1402017
Prevalence and correlates of gout in a large cohort of patients with chronic kidney disease: the German Chronic Kidney Disease (GCKD) study
J Jing, JT Kielstein, UT Schultheiss, T Sitter, SI Titze, ES Schaeffner, ...
Nephrology Dialysis Transplantation 30 (4), 613-621, 2015
1272015
A genome-wide association meta-analysis on lipoprotein (a) concentrations adjusted for apolipoprotein (a) isoforms [S]
S Mack, S Coassin, R Rueedi, NA Yousri, I Seppälä, C Gieger, ...
Journal of lipid research 58 (9), 1834-1844, 2017
1252017
Genetic studies of urinary metabolites illuminate mechanisms of detoxification and excretion in humans
P Schlosser, Y Li, P Sekula, J Raffler, F Grundner-Culemann, M Pietzner, ...
Nature genetics 52 (2), 167-176, 2020
1012020
Discontinuation versus continuation of renin-angiotensin-system inhibitors in COVID-19 (ACEI-COVID): a prospective, parallel group, randomised, controlled, open-label trial
A Bauer, M Schreinlechner, N Sappler, T Dolejsi, H Tilg, BA Aulinger, ...
The Lancet Respiratory Medicine 9 (8), 863-872, 2021
932021
A high-resolution HLA reference panel capturing global population diversity enables multi-ancestry fine-mapping in HIV host response
Y Luo, M Kanai, W Choi, X Li, S Sakaue, K Yamamoto, K Ogawa, ...
NATURE GENETICS, 2021
832021
Experiences with workflows for automating data-intensive bioinformatics
O Spjuth, E Bongcam-Rudloff, GC Hernández, L Forer, M Giovacchini, ...
Biology direct 10 (1), 1-12, 2015
822015
Genetic risk variants for membranous nephropathy: extension of and association with other chronic kidney disease aetiologies
P Sekula, Y Li, HC Stanescu, M Wuttke, AB Ekici, D Bockenhauer, G Walz, ...
Nephrology Dialysis Transplantation 32 (2), 325-332, 2017
792017
A novel but frequent variant in LPA KIV-2 is associated with a pronounced Lp(a) and cardiovascular risk reduction
S Coassin, G Erhart, H Weissensteiner, M Eca Guimarães de Araújo, ...
European heart journal 38 (23), 1823-1831, 2017
772017
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